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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423964Generated: October 29, 2026

2-Chloro-1-(piperidin-1-yl)propan-1-one → 6-{2-{Ethyl[4-(1-methyl-2-piperidin-1-ylethoxy)benzyl]amino}-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-ol

https://huagongshe.com/reaction/2423964

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1-(piperidin-1-yl)propan-1-oneHCID 3282976—
ReactantPivalic acid 6-{2-[ethyl(4-hydroxybenzoyl)amino]-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-yl esterHCID 57934562—
Product6-{2-{Ethyl[4-(1-methyl-2-piperidin-1-ylethoxy)benzyl]amino}-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-olHCID 5793424242.5%

Reaction Steps

Synthesized from pivalic acid 6-{2-[ethyl(4-hydroxybenzoyl)amino]-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-yl ester (29 mg) and 2-chloro-1-piperidin-1-ylpropan-1-one (20 mg) according to an analogous synthetic method to Example 404 and purified by LC-MS, the title compound (13 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960412B2
Source datasetuspto-grants-2011_06
ORD IDord-e0f1cbd004a54f68b537b4ea56ca5627
Source noteuspto-grants-2011_06